|Publication number||US5577509 A|
|Application number||US 08/189,000|
|Publication date||Nov 26, 1996|
|Filing date||Jan 28, 1994|
|Priority date||Jan 28, 1994|
|Also published as||WO1995020347A1|
|Publication number||08189000, 189000, US 5577509 A, US 5577509A, US-A-5577509, US5577509 A, US5577509A|
|Inventors||Dorin N. Panescu, David K. Swanson, Mark S. Mirotznik, David S. Schwartzman|
|Original Assignee||Ep Technologies, Inc.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (38), Non-Patent Citations (2), Referenced by (20), Classifications (33), Legal Events (5)|
|External Links: USPTO, USPTO Assignment, Espacenet|
The invention relates to systems and methods for mapping the interior regions of the heart for treatment of cardiac conditions.
Physicians examine the propagation of electrical impulses in heart tissue to locate aberrant conductive pathways. The aberrant conductive pathways constitute peculiar and life threatening patterns, called dysrhythmias. The techniques used to analyze these pathways, commonly called "mapping," identify regions in the heart tissue, called foci, which are ablated to treat the dysrhythmia.
Conventional cardiac tissue mapping techniques use multiple electrodes positioned in contact with epicardial heart tissue to obtain multiple electrograms. Digital signal processing algorithms convert the electrogram morphologies into isochronal displays, which depict the propagation of electrical impulses in heart tissue over time. These conventional mapping techniques require invasive open heart surgical techniques to position the electrodes on the epicardial surface of the heart.
Furthermore, conventional epicardial electrogram processing techniques used for detecting local electrical events in heart tissue are often unable to interpret electrograms with multiple morphologies. Such electrograms are encountered, for example, when mapping a heart undergoing ventricular tachycardia (VT). For this and other reasons, consistently high correct foci identification rates (CIR) cannot be achieved with current multi-electrode mapping technologies.
Researchers have taken epicardial measurements of the electrical resistivity of heart tissue. Their research indicates that the electrical resistivity of infarcted heart tissue is about one-half that of healthy heart tissue. Their research also indicates that ischemic tissue occupying the border zone between infarcted tissue and healthy tissue has an electrical resistivity that is about two-thirds that of healthy heart tissue. See, e.g., Fallert et al., "Myocardial Electrical Impedance Mapping of Ischemic Sheep Hearts and Healing Aneurysms," Circulation, Vol. 87, No. 1, January 1993 , 199-207.
This observed physiological phenomenon, when coupled with effective, non-intrusive measurement techniques, can lead to cardiac mapping systems and procedures with a CIR better than conventional mapping technologies.
A principal objective of the invention is to provide improved probes and methodologies to examine heart tissue morphology quickly, accurately, and in a relatively non-invasive manner.
One aspect of the invention provides systems and methods for examining heart tissue morphology using a pair of electrodes,at least one of which is located in contact with heart tissue. The systems and methods transmit electrical current in a path through the contacted heart tissue between the pair of the electrodes to derive a tissue electrical characteristic based, at least in part, upon sensing the impedance of the tissue lying in the path. The system and methods also sense with at least one of the electrodes the timing of local depolarization events in the contacted heart tissue.
The electrical characteristic (called the "E-Characteristic") can be directly correlated to tissue morphology. A low relative E-Characteristic indicates infarcted heart tissue, while a high relative E-Characteristic indicates healthy heart tissue. Intermediate E-Characteristic values indicate the border of ischemic tissue between infarcted and healthy tissue.
The timing of local depolarization events offer another indication of the electro-physiological morphology of the tissue. Used in tandem, these two characteristics can be used to assess the morphology of heart tissue.
In a preferred embodiment, the systems and methods generate a first output indicative of the derived E-Characteristic while generating a second output indicative if the sensed timing of local depolarization events.
In a preferred embodiment, the first output is a display showing the derived E-Characteristic in spatial relation to the location of the examined tissue regions. In this arrangement, the second output arranges the sensed local depolarization events into groups of equal timing and generates an output of the groups of equal timing in spatial relation to the location of the multiple paths in the region. This output can comprise either an isochronal output or an iso-delay output.
In this way, the invention makes possible the coordinated mapping of the E-Characteristic and local depolarization events in heart tissue to aid in the identification of possible tissue ablation sites.
How the E-Characteristic is expressed depends upon how the electrical current is transmitted by the electrode pair through the heart tissue.
When one of the electrodes in the pair comprises an indifferent electrode located outside the heart (i.e., a unipolar arrangement), the E-Characteristic is expressed in terms of tissue impedance (in ohms). When both electrodes in the pair are located inside the heart (i.e., a bipolar arrangement), the E-Characteristic is expressed in terms of tissue resistivity (in ohm·cm).
In a preferred embodiment, the systems and methods employ electrodes carried by catheters for introduction into contact with endocardial tissue through a selected vein or artery. The systems and methods transmit electric current and process information through signal wires carried by the electrodes. The electrodes can be connected to a multiplexer/demultiplexer element, at least a portion of which is carried by the catheter, to reduce the number of signal wires the catheter carries, and to improve the signal-to-noise ratio of the data acquisition system.
Other features and advantages of the inventions are set forth in the following Description and Drawings, as well as in the appended Claims.
FIG. 1 is a plan view, with portions in section, of a system for examining and mapping heart tissue morphology according to the features of the invention, shown deployed for use within the heart;
FIG. 2 is a plan view, with portions in section, of the system shown in FIG. 1 in the process of being deployed for use within the heart;
FIG. 3 is a view of the mapping probe and process controller associated with the system shown in FIG. 1;
FIG. 4 is an enlarged perspective view of an electrode carrying spline associated with the probe shown in FIG. 1;
FIG. 5 is a cross sectional view of an alternative embodiment of an electrode that can be associated with the probe shown in FIG. 1, taken generally along line 5--5 in FIG. 6;
FIG. 6 is an enlarged perspective view of an alternative embodiment of an electrode carrying spline that can be associated with the probe shown in FIG. 1;
FIGS. 6A to 6C and associated catheter tube are views of a flexible electrode support body that can carry the electrodes and deployed in the heart according to the invention;
FIG. 7 is a schematic view of the current generator module and switching element of the process controller for the system shown in FIG. 1;
FIG. 8 is a diagrammatic view of the current generator module and switching element when operated in a Unipolar Mode;
FIG. 9 is a diagrammatic view of the current generator module and switching element when operated in a Bipolar Two Electrode Mode;
FIG. 10 is a diagrammatic view of the current generator module and switching element when operated in a Bipolar Four Electrode Mode;
FIGS. 11 and 12 are schematic views of the details of the switching element shown in FIGS. 7 to 10;
FIG. 13 is a schematic view of the signal processor module of the process controller for the system shown in FIG. 1;
FIG. 14 is a schematic view of the E-Characteristic computing system of the signal processor module shown in FIG. 13;
FIG. 15 is an illustrative, idealized display of the absolute tissue E-Characteristic values derived by the system shown in FIG. 14 arranged in spatial relation to a region of the heart;
FIG. 16 is a flow chart showing the operation of the system that arranges the derived absolute tissue E-Characteristic values into groups of equal values;
FIG. 17 is a representative display of the groups of equal E-Characteristic values derived by the system shown in FIG. 16 arranged in spatial relation to a region of the heart; and
FIG. 18 is a diagrammatic view of an alternative embodiment of a controller that can be used in association with the system shown in FIG. 1;
FIG. 19 is a diagrammatic view of the pacing module that the controller shown in FIG. 18 includes;
FIG. 20 is a diagrammatic view of the host processing unit and electrogram signal processing module with which the controller shown in FIG. 18 is associated;
FIG. 21A is a view of four representative electrograms that can be used to compute electrogram events;
FIG. 21B is a flow chart showing the methodology for computing an electrogram event for processing by the controller shown in FIG. 18;
FIG. 22 is a flow chart showing the operation of the means for constructing an iso-display of the computed electrogram event;
FIG. 23 is a representative iso-chronal display;
FIG. 24 is a flow chart showing the operation of the means for constructing an iso-conduction display of the computed electrogram event;
FIG. 25 is a representative iso-conduction display;
FIG. 26 is a flow chart showing the operation of the means for matching iso-E-Characteristics with iso-conduction information;
FIG. 27 is a representative display of the matched iso-E-Characteristics and iso-conduction information;
FIG. 28 is a flow chart showing the operation of the means for detecting a possible ablation site based upon the information obtain in FIG. 26;
FIG. 29 is a representative display of the matched Iso-E-Characteristics and iso-conduction information, after selection of a threshold value, identifying a potential ablation site; and
FIG. 30 is a plan view of an ablation probe being used in association with the system shown in FIG. 1.
The invention may be embodied in several forms without departing from its spirit or essential characteristics. The scope of the invention is defined in the appended claims, rather than in the specific description preceding them. All embodiments that fall within the meaning and range of equivalency of the claims are therefore intended to be embraced by the claims.
FIGS. 1 to 3 show the components of a system 10 for examining heart tissue morphology. FIG. 1 shows the system 10 deployed and ready for use within a selected region 12 inside a human heart.
As FIGS. 1 and 2 show, deployment of the system 10 does not require invasive open heart surgical techniques. Instead, the system 10 includes an introducer 14 and an outer guide sheath 16 that together direct a multiple electrode probe 18 into the selected region 12 within the heart through a selected vein or artery. FIG. 3 shows the probe 18 in its entirety.
The physician uses the probe 18 in association with a process controller 20 (see FIG. 3) to take multiple, sequential measurements of the transmission of electrical current by heart tissue. From these, the E-Characteristic of the tissue is derived. In the illustrated and preferred embodiment, these measurements are used to assist the physician in identifying appropriate ablation sites within the heart.
FIG. 1 and the other figures generally show the system 10 deployed in the left ventricle of the heart. Of course, the system 10 can be deployed in other regions of the heart, too. It should also be noted that the heart shown in the Figures is not anatomically accurate. The Figures show the heart in diagrammatic form to demonstrate the features of the invention.
I. NON-INVASIVE SYSTEM DEPLOYMENT
As FIG. 1 shows, the introducer 14 has a skin-piercing cannula 22. The cannula 22 establishes percutaneous access into the selected vein or artery (which is typically the femoral vein or artery). The other end of the introducer 14 includes a conventional hemostatic valve 24.
The physician advances the outer guide sheath 16 through the introducer 14 through the vein or artery into the selected heart chamber 12. The hemostatic valve 24 yields to permit the introduction of the outer guide sheath 16 through it, but otherwise conforms about the outer surface of the sheath 16, thereby maintaining a fluid tight seal.
Preferably, the guide sheath 16 includes a precurved distal tip region 26, like a conventional "pig tail" catheter. The precurved distal tip region 26 assists in steering the guide sheath 16 into position within the heart chamber 12.
The physician advances the probe 18 through the handle 28 of the outer sheath 16. The handle 28 includes a second conventional hemostatic valve 30 that yields to permit the introduction of the flexible body 32 of the mapping probe 18 through it. At the same time, the valve 30 conforms about the outer surface of the body 22 to maintain a fluid tight seal.
Further details of the deployment and use of the introducer 14 and guide sheath 16 to establish a pathway for the probe 18 are set forth in pending U.S. patent application Ser. No. 08/033,641, filed Mar. 16, 1993, entitled "Systems and Methods Using Guide Sheaths for Introducing, Deploying, and Stabilizing Cardiac Mapping and Ablation Probes."
II. THE TISSUE EXAMINATION PROBE
As FIGS. 1 and 3 best show, the probe 18 has a handle 34 attached to the proximal end of the flexible catheter body 32. The distal end of the catheter body 32 carries a three dimensional structure 36. In FIGS. 1 and 3, the structure 36 takes the form of a basket. It should be appreciated that other three dimensional structures could be used.
The three dimensional basket structure 36 carries an array of electrodes 38.
As FIG. 1 shows, when deployed inside the heart chamber 12, the basket structure 36 holds the electrodes 38 in intimate contact against the endocardial surface of the heart chamber 12.
The catheter body 32 passes through the outer guide sheath 16. The sheath 16 has an inner diameter that is greater than the outer diameter of the catheter body 32. As a result, the sheath 16 can slide along the catheter body 32. The sheath handle 28 helps the user slide the sheath 16 along the catheter body 32.
As FIG. 2 shows, forward movement of the sheath handle 28 (i.e., toward the introducer 14) advances the distal end of the slidable sheath 16 upon the basket structure 36. In this position, the slidable sheath 16 captures and collapses the basket structure 36, entirely enclosing the basket structure 36.
As FIG. 1 shows, rearward movement of the sheath handle 28 (i.e., away from the introducer 14) retracts the slidable sheath 16 away from the basket structure 36. This removes the compression force, and the basket structure 36 opens to assume its prescribed three dimensional shape.
The probe 18 also preferably includes a sliding hemostat sheath 40. The physician slides the sheath 40 about the basket structure 36 to protect it during its advancement through the introducer 14. Once the basket structure 36 enters the guide sheath 16, the physician slides the hemostatic sheath 40 away rearward toward the probe handle 34. Further details of the use of the sheath 40 are disclosed in the above-identified pending Patent Application.
The basket structure 36 can itself be variously constructed. In the illustrated and preferred embodiment (see FIG. 3), the basket structure 36 comprises a base member 42 and an end cap 44. Generally flexible splines 46 extend in a circumferentially spaced relationship between the base member 42 and the end cap 44.
In the illustrated embodiment, eight, rectilinear splines 46 form the basket structure 36. However, additional or fewer splines 46 could be used, as could spline of different configurations.
In this arrangement, the splines 46 are preferably made of a resilient inert material, like Nitinol metal or silicone rubber. The splines 46 are connected between the base member 42 and the end cap 44 in a resilient, pretensed condition, shown in FIG. 3.
As FIG. 1 shows, the resilient splines 46 bend and conform to the endocardial tissue surface they contact. As FIG. 2 shows, the splines 46 also collapse into a closed, compact bundle in response to the external compression force of the sliding sheath 18.
In the illustrated embodiment (see FIG. 4), each spline 46 carries eight electrodes 38. Of course, additional or fewer electrodes 38 can be used.
As will be described later, the system 10 can be operated in either a unipolar mode or a bipolar mode. The basket electrodes 38 can therefore be arranged in thirty-two bi-polar pairs, or as sixty-four uni-polar elements.
In the illustrated and preferred embodiment (as FIG. 4 best shows), the electrodes 38 are mounted to each spline 46 to maximize surface contact to endocardial tissue, while at the same time minimizing exposure to the surrounding blood pool. Incidental exposure of the electrodes 38 to blood while in contact with heart tissue introduces an unwanted artifact to E-Characteristic measurement, because the resistivity of blood is about three times lower than the resistivity of heart tissue. This artifact can skew the E-Characteristic measurement to a lower value, thereby reducing the desired contrast between healthy and infarcted tissue.
In the preferred embodiment (see FIG. 4), the electrodes 38 are made of platinum or gold plated stainless steel bands affixed to only one side of the splines 46. This is the side of the spline 46 that, in use, contacts endocardial tissue. The opposite surface of the splines 46 (which, in use, contacts the blood pool) is free of electrodes.
In an alternative arrangement (see FIGS. 5 and 6), the electrodes 38 can take the form of rings that encircle the entire spline 46. In this arrangement, the rear side of the electrodes 38, which during use face the blood pool, are coated with an electrically insulating material 49 to prevent current transmission into blood.
It is believed that no more than 20% of the electrode surface should be exposed to the blood pool during use. Preferable, less than 5% of the electrode should be so exposed during use.
In an alternative arrangement (see FIGS. 6A to 6C), one or more of electrodes 38 can be introduced into the heart chamber through a vein or artery on a single flexible electrode support body 300, and not on a basket structure like that earlier described. The body 300 is illustrative of a family of flexible, elongated electrode supports of various alternative constructions. In the preferred and illustrated embodiment, the body 300 is about 1 to 2.5 mm in diameter and about 1 to 5 cm long.
As FIG. 27 shows, the body 300 is carried at the distal end of a catheter tube 302 used to guide the body 300 into the heart. A handle 304 is attached to the proximal end of the catheter tube 302. The handle 304 and catheter tube 302 carry a steering mechanism 306 for selectively bending or flexing the support body 300 along its length, as the arrows in FIG. 6A show.
The steering mechanism 306 can vary. In the illustrated embodiment (see FIG. 6C), the steering mechanism 306 includes a rotating cam wheel 308 with an external steering lever 310 (as FIG. 6A shows). As FIG. 6C shows, the cam wheel 308 holds the proximal ends of right and left steering wires 312. The wires 312 pass through the catheter tube 302 and connect to the left and right sides of a resilient bendable wire or spring (not shown) within the ablating element support body 300.
As FIG. 6A shows, movement of the steering lever 310 flexes or curves the support body 300 from a generally straight configuration (shown in phantom lines in FIGS. 6A and 6B) into a generally arcuate curve (shown in solid lines in FIGS. 6A and 6B). Through flexing, the electrodes 38 can also be brought into conforming, intimate contact against the endocardial tissue, despite the particular contours and geometry that the wall presents.
As shown in FIG. 6B, the electrodes 38 comprise rings encircling the support body 300. In this arrangement, the rear sides of the electrodes 38, which, in use, face the blood pool, are preferably coated with the electrical insulating material 49 for the reasons stated above. Alternatively, the electrodes 38 can be affixed only to the tissue-contacting side of the support body 300, thereby making the rear side of the support body 300 free of electrodes 38, like the rectilinear spline 46 shown in FIG. 4.
The electrodes 38 carried by the support body 300, as FIG. 6B shows, can by used in association with the process controller 20 to take one or more E-Characteristic measurements, just as the electrodes carried by the basket structure. The support body 300 can be moved sequentially to different endocardial sites to obtain a plurality of E-Characteristic measurements, which can be processed in the same manner as those taken by the stationary basket structure.
Further details of flexible electrode carrying elements can be found in copending U.S. patent application Ser. No. 08/138,142, filed Oct. 15, 1993, entitled "Systems and Methods for Creating Long, Thin Lesions in Body Tissue."
In the illustrated embodiments (see FIGS. 4 and 6), a signal wire 47 made from a highly conductive metal, like copper, leads from each electrode 46 (these signal wires are also shown diagrammatically in FIG. 11). The signal wires 47 extend down the associated spline 46, by the base member 42, and into the catheter body 32. An inert plastic wrapping 43 preferably covers each spline 46 and electrode support body 300, except where the electrodes 38 project, to shield the signal wires.
The eight signal wires 47 for each spline 46 are twisted together to form a common bundle. The eight common bundles (not shown) are, in turn, passed through the catheter body 32 of the mapping probe 18. The common bundles enter the probe handle 34.
The sixty-four signal wires 47 are connected within the probe handle 34 to one or more external connectors 48, as FIG. 3 shows. In the illustrated embodiment, each connector contains thirty-two pins to service thirty-two signal wires.
In an alternative arrangement (not shown), the electrodes 38 can be connected to a multiplexer/demultiplexer (M/DMUX) block (not shown) to reduce the number of signal wires carried by the catheter body 32. The M/DMUX block can comprise a multi-die integrated circuit mounted on a flexible support and wrapped about the catheter body 32. The signal-to-noise-ratio is thereby improved.
III. MEASURING AND MAPPING THE TISSUE E-CHARACTERISTIC
The system 10 transmits electrical current in a selected manner through the basket electrodes 38 in contact with endocardial tissue. From this, the system 10 acquires impedance information about the heart tissue region that the basket electrodes 38 contact. The system 10 processes the impedance information to derive the E-Characteristic, which assists the physician in identifying regions of infarcted tissue where ablation therapy may be appropriate.
For these purposes (see FIG. 3), the system 10 includes the process controller 20. The process controller 20 includes a current generator module 50 and a signal processor module 52. The connectors 48 electrically couple the basket electrodes 38 to both the generator module 50 and the processor module 52.
A. The Current Generator Module
The generator module 50 conveys a prescribed current signal to individual basket electrodes 38.
In the illustrated and preferred embodiment (see FIG. 7), the generator module 50 includes an oscillator 54 that generates a sinusoidal voltage signal. An associated interface 56 has a bus 58 that controls the frequency of the output voltage signal and a bus 60 that controls the amplitude of the output voltage signal. The interface 56, in turn, is programmed by a host processor 206, which will be described in greater detail later.
The oscillator 54 has as an output stage that includes a voltage-to-current converter 62. In conventional fashion, the converter 62 converts the sinusoidal voltage signal to current.
In the illustrated and preferred embodiment, the transmitted current has an amplitude of about 0.1 milliamps to 5.0 milliamps. The lower range of the current amplitude is selected to be high enough to overcome the influence of the double layer at the tissue-electrode interface on the E-Characteristic measurement. The high range of the current amplitude is selected to avoid the induction of fibrillation.
The current has a frequency in a range of about 5 to 50 kHz. The range is selected to avoid the induction of fibrillation, as well as provide contrast between infarcted tissue and healthy tissue. The output of the converter 62 can comprise a constant current with a constant frequency within the above range. Alternatively, the interface 56 can control the modulation of the frequency of the current signal within the prescribed range. Deriving tissue E-Characteristic by transmitting currents with different frequencies better differentiates among different tissue morphologies. It has been determined that lower frequencies within the range provide E-Characteristics yielding greater quantitative contrast between infarcted and healthy tissues than higher frequencies in this range.
The current output of the module 50 is supplied to the basket electrodes 38 via supply path 68 through a switching element 64. The interface 56 electronically configures the switching element 64 to direct current in succession to selected basket electrodes 38 through their associated signal wires in either a unipolar mode or a bipolar mode. Line 66 constitutes the control bus for the switching element 64.
As FIG. 8 shows, when operated in a unipolar mode, the current return path 70 to the generator module 50 is provided by an exterior indifferent electrode 72 attached to the patient.
When operated in a bipolar mode, the current return path 70 is provided by an electrode carried on the basket structure 36 itself. In the illustrated and preferred embodiment, the bipolar return electrode is either located immediately next to or three electrodes away from the selected transmitting basket electrode along the same spline. The first circumstance (shown in FIG. 9) will be called the Bipolar Two Electrode Mode. The second circumstance (shown in FIG. 10) will be called the Bipolar Four Electrode Mode.
The configuration of the switching element 64 can vary. FIG. 11 diagrammatically shows one preferred arrangement.
FIG. 11 shows for illustration purposes a spline 46 with seven adjacent electrodes 38, designated E1 to E7. Each electrode E1 to E7 is electrically coupled to its own signal wire, designated W1 to W7. The indifferent electrode, designated EI in FIG. 11, is also electrically coupled to its own signal wire WI.
In this arrangement, the switching element 64 includes an electronic switch SM and electronic switches SE1 to SE7 that electrically couple the current generator to the signal wires W1 to W7. The switch SM governs the overall operating mode of the electrodes E1 to E7 (i.e., unipolar or bipolar). The switches SE1 to SE7 govern the electrical conduction pattern of the electrodes E1 to E7.
The switches SM and SE1 to E7 are electrically coupled to the current source. The supply path 68 of the generator module 50 is electrically coupled to the leads L1 of the switches SE1 to E7. The return path 70 of the generator module 50 is electrically coupled to the center lead L2 of the mode selection switch SM. A connector 67 electrically couples the leads L3 of the switches SM and SE1 to E7.
The center leads L2 of the selecting switches SE1 to E7 are directly electrically coupled to the signal wires W1 to W7 serving the electrodes E1 to E7, so that one switch SE(N) serves only one electrode E.sub.(N).
The lead L1 of the switch SM is directly electrically coupled to the signal wire WI serving the indifferent electrode EI.
The interface 56 electronically sets the switches SM and SE1 to E7 among three positions, designated A, B, and C in FIG. 12.
As FIG. 12 shows, Position A electrically couples leads L1 and L2 of the associated switch. Position C electrically couples leads L2 and L3 of the associated switch. Position B electrically isolates both leads L1 and L3 from lead L2 of the associated switch.
Position B is an electrically OFF position. Positions A and B are electrically ON positions.
By setting switch SM in Position B, the interface 56 electronically inactivates the switching network 54.
By setting switch SM in Position A, the interface 56 electronically configures the switching element for operation in the unipolar mode. The center lead L2 of switch SM is coupled to lead L1, electronically coupling the indifferent electrode EI to the return of the current generator. This configures the indifferent electrode EI as a return path for current.
With switch SM set in Position A, the interface 56 electronically selectively configures each individual electrode E1 to E7 to emit current by sequentially setting the associated switch SE1 to E7 in Position A. When the selected electrode E1 to E7 is so configured, it is electronically coupled to the supply of the current generator and emits current. The indifferent electrode EI receives the current sequentially emitted by the selected electrode E1 to E7.
By setting switch SM in Position C, the interface 56 electronically isolates the indifferent electrode EI from the electrodes E1 to E7. This configures the switching element for operation in the bipolar mode.
With switch SM set in Position C, the interface 56 can electronically alter the polarity of adjacent electrodes E1 to E7, choosing among current source, current sink, or neither.
By setting the selected switch SE1 to E7 in Position A, the interface 56 electronically configures the associated electrode E1 to E7 to be a current source. By setting the selected switch SE1 to E7 in Position C, the interface 56 electronically configures the associated electrode E1 to E7 to be a current sink. By setting the selected switch SE1 to E7 in Position B, the interface 56 electronically turns off the associated electrode E1 to E7.
In the Bipolar Two Electrode Mode, the interface 56 first configures the electrode E1 to be a current source, while configuring the immediate adjacent electrode E2 to be a current sink, while turning off the remaining electrodes E3 to E7. After a preselected time period, the interface 56 then turns off electrode E1, configures electrode E2 to be a current source, configures the next immediate adjacent electrode E3 to be a current sink, while keeping the remaining electrodes E4 to E7 turned off. After a preselected time period, the interface 56 then turns off electrode E2, configures electrode E3 to be a current source, configures the next immediate adjacent electrode E4 to be a current sink, while keeping the remaining electrodes E1 and E5 to E7 turned off. The interface 56 cycles in this timed sequence until electrodes E6 and E7 become the current source/sink bipolar pairs (the remaining electrodes E1 to E5 being turned off). The cycle can then be repeated, if desired, or ended after one iteration.
In the Bipolar Four Electrode Mode, the interface 56 first configures the electrode E1 to be a current source, while configuring the third adjacent electrode E4 to be a current sink, while turning off the remaining electrodes E2, E3, and E5 to E7. After a predetermined time period, the interface 56 turns off electrode E1, configures electrode E2 to be a current source, configures the next third adjacent electrode E5 to be a current sink, while keeping the remaining electrodes E3, E4, E6, and E7 turned off. After a predetermined time period, the interface 56 turns off electrode E2, configures electrode E3 to be a current source, configures the next third adjacent electrode E6 to be a current sink, while keeping the remaining electrodes E1, E2, E4, E5, and E7 turned off. The interface 56 cycles in this timed sequence until electrodes E4 and E7 become the current source/sink bipolar pairs (the remaining electrodes E1 to E3, E5, and E6 being turned off. The cycle can then be repeated, if desired, or ended after one iteration.
In the preferred embodiment, there is a switching element 64 for the electrodes on each basket spline, with the interface 56 independently controlling each switching element.
B. Computing Tissue E-Characteristic
As FIG. 13 shows, the signal processor module 52 includes a data acquisition system 74. While current is emitting by a selected basket electrode, the system 74 senses the voltage in the tissue path using selected electrodes on the basket 36.
Based upon the data acquired by the system 74, the host processor 206 computes the E-Characteristic of the tissue path as follows:
(1) When operated in the Unipolar Mode, the E-Characteristic is the impedance of the tissue path, computed based upon the following equation: ##EQU1##
The PathVoltage and PathCurrent are both root mean squared (RMS) values.
In the unipolar mode (see FIG. 8), the voltage is measured between each transmitting electrode and the indifferent electrode (or between EI and E(n), where n represents the location of the current emitting electrode). The impedance computed by the host processor 206 in this mode reflects not only the impedance of the underlying myocardial tissue, but also includes the impedance of the other tissue mass in the path. The computed impedance in this mode therefore is not the actual impedance of the myocardial tissue itself. Rather, it provides a relative scale of impedance (or E-Characteristic) differences of the myocardial tissue lying in contact with the spline electrodes.
(2) When operated in the Bipolar Mode, the ##EQU2## E-Characteristic of the tissue is the resistivity of the tissue path, computed as follows:
Resistivity (ohm·cm)=Impedance (ohm)×k(cm)
where k is a dimensional constant (in cm) whose value takes into account the methodology employed (i.e. either Bipolar Two Electrode Mode or Bipolar Four Electrode Mode) and the geometry of the electrode array (i.e., the size and spacing of the electrodes).
In general, k is approximately equal to the average cross sectional area of the current path divided by the distance between the voltage sensing electrodes. The accuracy of the k value can be further improved, if desired, empirically or by modeling.
The PathVoltage and PathCurrent are both root mean squared (RMS) values.
When operated in the Bipolar Two Electrode Mode (see FIG. 9), the voltage is measured between the two adjacent current emitting/receiving electrodes (or between E(n) and E(n+1)). When operated in the Bipolar Four Electrode Mode (see FIG. 10), the voltage is measured between the two adjacent electrodes lying in between the current transmitting electrode and the third adjacent return path electrode (or between E(n+1) and E(n+2)).
In either Bipolar Mode, the resistivity computed by the processor 206 reflects the actual resistivity of the myocardial tissue lying in contact with the spline electrodes. However, the Bipolar Two Electrode Mode is more prone to electric artifacts than the Bipolar Four Electrode Mode, such as those due to poor electrical contact between electrode and tissue.
As FIG. 14 shows, the voltage signals sensed by the basket electrodes 38 are passed back through the switching element 64 to the data acquisition system 74. As FIG. 11 shows, a signal conditioning element 224 preferably corrects alterations to the signal-to-noise ratio occurring in the voltage signals during propagation through the probe body 32.
The data acquisition system 74 includes a multiplexer 76 that selects and samples in succession the voltage associated with each transmitting electrode E(n) carried by the basket structure 36. For each selected current transmitting electrode E(n), the multiplexer 76 samples for a prescribed time period the analog sinusoidal voltage measured between the sensing electrodes.
A sample and hold element 80 stores the sampled analog voltage signals. The stored signals are sent to an analog-to-digital (A-to-D) converter 82, which converts the sampled voltage signals to digital signals. The multiplexer 76 makes possible the use of a single analog-to-digital conversion path.
The digital signals are sent to a host processor 206 through an interface 226. The host processor 206, based upon a conventional sorting scheme, obtains the peak voltage and, from that, computes the RMS voltage. The host processor 206 then computes the E-Characteristic, using the RMS voltage and RMS current (and, for the Bipolar Mode, the constant k) as described above. The RMS current is known by the processor 206, since it has been programmed by it through the interface 56 (see FIG. 7).
C. Processing the E-Characteristic
The computed E-Characteristic values can be processed by the system 10 in various ways.
In one embodiment (see FIG. 13), the signal processor module includes means 90 for sorting the multiple computed E-Characteristic values in absolute terms, arranging them according to a preassigned electrode numbering sequence, representing relative electrode position.
The means 90 can create as an output a table (either as a graphic display or in printed form), as follows:
TABLE 1______________________________________SPLINE ELECTRODE E-CHAR______________________________________S1 E1 75S1 E2 114S1 E3 68S1 E4 81S2 E1 69S2 E2 71S2 E3 67S2 E4 66S3 E1 123S3 E2 147S3 E3 148S3 E4 140. . . etc . . . . . . etc . . . . . . etc . . .______________________________________
In Table 1, the spline elements of the basket are identified as S1, S2, S3, etc. The electrodes carried by each spline element are numbered from the distal end as E1, E2, E3, and so on. The E-Characteristic values are expressed in terms of resistivity (ohm·cm). The values expressed are idealized and given for illustration purposes. In addition, or alternatively, the means 90 can also create as an output a two or three dimensional display that spatially maps the relative position of the computed absolute resistivity values, based upon basket electrode positions.
FIG. 15 shows a representative display of E-Characteristics (expressed as resistivity values), based upon the data listed in Table 1. In FIG. 15, circled Area A identifies a region of low relative tissue resistivity, indicative of infarcted heart tissue. Area B in FIG. 15 is a region of normal tissue resistivity, indicative of healthy heart tissue.
Preferably, the signal processor module 52 also includes means 92 (see FIG. 13) for arranging the derived absolute E-Characteristics into groups of equal E-Characteristic values for display in spatial relation to the location of the electrodes 38. This output better aids the physician in interpreting the E-Characteristics, to identify the regions of low relative tissue E-Characteristics, where ablation may be appropriate.
As FIG. 16 shows, the means 92 includes a processing step that computes the location of the electrodes 38 in a three dimensional coordinate system. In the illustrated and preferred embodiment, a three dimensional spherical coordinate system is used.
The means 92 next includes a processing step that generates by computer a three dimensional mesh upon the basket surface. The points where the mesh intersect are called nodes. Some of the nodes will overlie the electrodes on the basket. These represent knots, for which the values of the E-Characteristic are known.
The values of the E-Characteristic for the remaining nodes of the three dimensional mesh have not been directly measured. Still, these values can be interpolated at each remaining node based upon the known values at each knot.
One method of doing this interpolation is using three dimensional cubic spline interpolation, although other methods can be used. The cubic spline interpolation process is incorporated in the MATLAB™ program, sold by The MathWorks Incorporated.
The means 92 creates an output display by assigning one distinguishing idicium to the maximum E-Characteristic value (whether actually measured or interpolated) and another distinguishing idicium to the minimum E-Characteristic value (again, whether actually measured or interpolated). In the illustrated and preferred embodiment, the distinguishing indicia are contrasting colors or shades.
The means 92 assigns computer generated intermediate indicia to intermediate measured and interpolated values, based upon a linear scale. In the illustrated and preferred embodiment, the intermediate indicia are color hues between the two contrasting colors or shades.
The means 92 projects the generated color (or selected indicia) map upon the basket surface, based upon location of the nodes in the three dimensional mesh. The means 92 thus creates as an output a display showing iso-E-Characteristic regions.
FIG. 17 shows a representative display of iso-resistivity regions, based upon the idealized, illustrative data listed in Table 1.
D. Matching E-Characteristic and Tissue Conductivity
FIG. 18 shows another embodiment of a process controller 200 that can be used in association with the probe 18, as already described. The process controller 200 in FIG. 18, like the process controller 20 shown in FIG. 3, includes the current generator module 50 and the signal processing module 52 for deriving and processing tissue E-Characteristics in the manners previously discussed.
In addition, the process controller 200 in FIG. 18 includes a module 202 for pacing the heart to acquire electrograms in a conventional fashion. The pacing module 202 is electrically coupled to the probe connectors 48 to provide a pacing signal to one electrode 38, generating depolarization foci at selected sites within the heart. The basket electrodes 38 also serve to sense the resulting electrical events for the creation of electrograms.
Operation of the pacing module 202 is not required when ventricular tachycardia (VT) is either purposely induced (e.g., by programmed pacing) or occurs spontaneously. In this situation, the deployed basket electrodes 38 sense the electrical events associated with VT itself.
The process controller 200 in FIG. 18 further includes a second signal processing module 204 for processing the electrogram morphologies obtained from the basket electrodes 38.
The process controller 200 in FIG. 18 also includes a host processor 206 that receives input from the data acquisition system 74 and the electrogram processing module 204. The processor 206 analyzes the tissue E-Characteristic and electrogram information to compute a matched filtered output, which further enhances the CIR of ablation site identification.
The modules 202, 204, and 206 may be configured in various ways.
In the illustrated and preferred embodiment (see FIG. 19), the pacing module 202 includes a controller interface 208 coupled to the host processor 206, which will be described in greater detail later. The controller interface 208 is also coupled to pulse generator 210 and an output stage 212.
The output stage 212 is electrically coupled by supply path 220 and return path 218 to the same switching element 64 as the current generator module 50. The switching element 64 has been previously described and is shown schematically in FIG. 11. As FIG. 11 shows in phantom lines, the pacing module 202 and current generator module 50 are connected to the switching element 64.
The controller interface 208 includes control buses 214, 216, and 218. Bus 214 conveys pulse period control signals to the pulse generator 210. Bus 216 conveys pulse amplitude control signals to the pulse generator 210. Bus 219 constitutes the control bus path for the switching element 64.
When used to pace the heart, the switching element 64 distributes the signals generated by the pacing module 202 to selected basket electrodes 38. The pacing sequence is governed by the interface 208, which the host processor 206 controls.
The resulting electrogram signals sensed by the basket electrodes 38 are also passed back through the switching element 64 to the host processor 206 and the processing module 204 through the same analog processing path as the E-Characteristic signals, as FIG. 11 shows, and as already described.
FIG. 20 schematically shows the components of the host processor 206 and the electrogram processing module 204.
The host central processing unit (CPU) 206 communicates with a mass storage device 230 and an extended static RAM block 232. A user interactive interface 234 also communicates with the CPU 206.
As FIG. 20 shows, the interactive user interface 234 includes an input device 244 (for example, a key board or mouse) and an output display device 246 (for example, a graphics display monitor or CRT).
The CPU 206 also communicates with the current generator module 50; pacing module 202 and the interface 226 for the system 74, as previously described. In this way, the CPU 206 coordinates overall control functions for the system 10.
As FIG. 206 shows, the electrogram processing module 204 includes a bus 235 and a bus arbiter 236 that receive the digital output of the A-to-D converter 82 through the interface 226. The bus arbiter 236 arbitrates the distribution of the digital electrogram morphology signals to one or more digital signal processors 238, which also form a part of the processing module 204 and which also communicate with the CPU 206.
The illustrated and preferred embodiment employs four signal processors 238 operating concurrently, but different numbers of processors 238 can be used. If N is the total number of basket electrodes and M is the number of processors 238, then each processor 238 is responsible for processing the signals coming from N/M electrodes in the Unipolar Mode and N/(2M) electrodes in the Bipolar Two or Four Mode.
To speed up data processing, each processor 238 includes a static RAM block 240. The data is processed real-time and stored in the blocks 240.
The signal processors 238 include various means for processing the electrogram signals as follows:
(i) to detect the earliest depolarization event;
(ii) to construct from the electrogram signals iso-chronal or iso-delay maps of the depolarization wavefronts, depending upon how the electrograms are obtained, which can be presented on the display device 246 for viewing by the physician; and
(iii) to construct from the electrogram signals iso-conduction maps, which can also be presented on the display device 246 for viewing by the physician.
The CPU 206 employs additional means for processing the electrogram signals and the E-Characteristic signals as follows:
(iv) to match the iso-conduction maps with the iso-E-Characteristic maps, which can be presented on the display device 246 for viewing by the physician; and
(v) based upon the matched output of (iv), to identify a potential ablation site.
(i) Identifying the Earliest Depolarization Event
FIG. 21B shows the means 250 for detecting the early depolarization event.
The CPU 206 displays the electrograms on the display 246 of the interactive user interface 234 (see FIG. 21A). After analyzing the display 246, the physician can manually choose a reference time for conventional electrogram beat clustering purposes. The physician can use the mouse or a keyboard device 244 for this purpose.
In the situation where ventricular tachycardia is purposely induced or is occurring spontaneously, the electrogram beats are clustered relative to the reference time to compute the propagation time when an electrogram for ventricular tachycardia is sensed by each electrode 38. For all the beats in the selected cluster, the physician manually selects the earliest depolarization event for each electrode 38. The interactive interface 234 transmits the physician's choice to the host CPU 206, which creates a matrix of the computed propagation times.
In the situation where the heart is being paced by the module 202, the beats are clustered relative to the reference time for computing the activation delay for each electrogram. The activation delay is measured between the pacing pulse and the earliest depolarization event. For all the beats in the selected cluster, the physician manually selects the earliest depolarization event for each electrode 38. In this situation as before, the interactive interface 234 transmits the physician's choice to the host CPU 206, which creates a matrix of the computed activation delays.
FIG. 21A shows four representative electrograms of a heart undergoing VT. FIG. 21A shows the reference time selected for beat clustering purposes and the early depolarization events selected for the purpose of illustration. From this, the propagation times t1 ; t2 ; t3 ; t4 can be computed as the differences between the time of the depolarization event and the reference time in each electrogram.
(ii) Constructing an Iso-Chronal or Iso-Delay Displays
FIG. 22 shows the means 252 for creating either an iso-chronal display of the propagation times (when VT is induced or spontaneously occurs) or an iso-delay display of activation times (when the module 202 is used to pace the heart). For purposes of description, each will be called the "computed electrogram event."
The means 252 generally follows the same processing steps as the means 92 (see FIG. 16) for creating the iso-E-Characteristic display.
The means 252 includes a processing step that computes the location of the electrodes in a spherical coordinate system.
The means 252 next generates by computer a three dimensional mesh upon the basket surface. The points where the mesh intersect are called nodes. Some of the nodes overlie the electrodes on the basket. These represent knots, for which the values of the computed electrogram event are known.
The values of the computed electrogram event for the remaining nodes of the three dimensional mesh have not been directly measured. Still, these values can be interpolated at each remaining node based upon the known values at each knot.
As before, three dimensional cubic spline interpolation can be used, although other methods can be used.
The means 252 creates an output display on the device 246 by assigning one color the maximum value of the computed electrogram event (whether actually measured or interpolated) and another color to the minimum value of computed electrogram event (again, whether actually measured or interpolated). Computer generated intermediate hues between the two colors are assigned by the host CPU 206 to intermediate measured and interpolated values, based upon a linear scale.
The means 252 projects the generated color map upon the basket surface, based upon location of the nodes in the three dimensional mesh.
FIG. 23 shows a representative display generated according to this processing means. The CPU 206 generates this display on the display device 246 for viewing by the physician.
A potential ablation site can be identified at regions where a rapid transition of hues occurs. Area A on FIG. 23 shows such a region.
When the electrograms used for beat clustering show an induced or spontaneous VT, the resulting display is an iso-chronal map of the examined tissue region. When the electrograms used for beat clustering are based upon a paced heart, the display is an iso-delay map of the examined tissue region.
(iii) Creating Iso-Conduction Display
FIG. 24 shows the means 254 for creating an iso-conduction displays of the computed electrogram event.
An iso-conduction display more rapidly identifies the regions of slow conduction which are candidate ablation sites, than an iso-chronal or iso-delay display. The iso-conduction display requires less subjective interpretation by the physician, as the regions of slow conduction stand out in much greater contrast than on an iso-chronal or iso-delay display.
The means 254 draws upon the same input and follows much of the same processing steps as the means 252 just described. The means 254 computes the location of the electrodes in a spherical coordinate system and then generates a three dimensional mesh upon the basket surface. The means 254 interpolates the computed electrogram event for the nodes based upon the known values at the knots.
Unlike the previously described means 252, the means 254 computes the inverse of the magnitude of the spatial gradient of the computed electrogram event. This inverse spatial gradient represents the value of the conduction of the cardiac signal in the examined tissue.
To carry out this processing step, the means 254 first computes the spatial gradient computed electrogram event for each node of the mesh. The methodology for making this computation is well known.
Next, the means 254 computes the magnitude of the spatial gradient, using, for example, known three dimensional vector analysis. Then, the means 254 computes the inverse of the magnitude, which represents the conduction value.
The means 254 clips all magnitudes larger than a predetermined threshold value, making them equal to the threshold value. This processing step reduces the effects of inaccuracies that may arise during the mathematical approximation process.
The computation of conduction (i.e., the velocity of the propagation) can be exemplified for the case when propagation times are processed. By substituting the activation delays for propagation times, one can compute the conductions for data obtained from paced hearts.
The location of any point on the three-dimensional mesh shown in FIG. 25 is given by the azimuth angle, φ and the elevation angle, δ. The radius of the underlying surface is normalized to one. The conduction is defined by EQUATION (1): ##EQU3##
Given that the radius of the meshed surface is one, one obtains the spatial gradient of propagation times: ##EQU4## where Φ and Δ are unity vectors of the spherical coordinate system defining the directions of the azimuth and elevation, respectively.
Thus, the conduction can be computed using EQUATION (3): ##EQU5## which is actually the inverse of the spatial gradient magnitude. When the conduction is numerically approximated, the derivatives in EQUATION (3) can be computed by any numerical method appropriate for the estimation of first derivatives.
The means 254 creates a display by assigning one color the threshold conduction value (i.e., the maximum permitted value) and another color to the minimum conduction value. Computer generated hues are assigned to intermediate values, based upon a linear scale, as above described.
The means 254 projects the generated color map upon the basket surface, based upon location of the nodes in the three dimensional mesh.
FIG. 25 shows a representative iso-conduction display generated according to the just described methodology and using the same data as the iso-chronal display shown in FIG. 23. The CPU 206 generates this display on the display device 246 for viewing by the physician.
Area A in FIG. 25 shows a region of slow conduction, which appears generally at the same location as the rapid hue transition in FIG. 23 (also identified as Area A). FIG. 25 shows the more pronounced contrast of the region that the iso-conduction display provides, when compared to the iso-chronal display of FIG. 23. Thus, the iso-conduction display leads to a more certain identification of a potential ablation site.
(iv) Matching Iso-Conduction with Iso-E-Characteristic
FIG. 26 shows the means 256 for matching the iso-conduction with the iso-E-Characteristic for the analyzed heart tissue.
The means 256 derives the values of the E-Characteristic at the nodes of three dimensional mesh in the same manner already described. Next, the means 256 normalizes these E-Characteristic values into an array of numbers from 0.0 to 1.0. The number 1.0 is assigned to the absolute lowest E-Characteristic value, and the number 0.0 is assigned to the absolute highest E-Characteristic value. E-Characteristic values between the absolute lowest and highest values are assigned numbers on a linear scale between the lowest and highest values.
The means 256 also derives the values of the computed electrogram event at the nodes of three dimensional mesh in the manner already described. The means 256 computes the inverse of the magnitude of spatial gradient of the computed electrogram event, as previously described, to derive the value of the conduction of the cardiac signal in the examined tissue.
The means 256 then normalizes these conduction values into an array of numbers from 0.0 to 1.0. The number 1.0 is assigned to the absolute lowest conduction value, and the number 0.0 is assigned to the threshold conduction value. As before, conduction values between the absolute lowest and highest values are assigned numbers on a linear scale between the lowest and highest values.
The means 256 then applies, using known mathematical computational techniques, a two dimensional matched filtering process to the normalized conduction data using the normalized E-Characteristic data as a template, or vice versa. Alternatively, a two dimensional cross-correlation can be applied to the normalized E-Characteristic and conduction. As used in this Specification, "matching" encompasses both two dimensional matched filtering, two dimensional cross-correlation, and a like digital signal processing techniques.
The values obtained from the matched filtering process are normalized, by dividing each value by the maximum absolute value. After normalization, the value will range between 0.0 and 1.0.
The means 256 creates a display by assigning one color the highest normalized matched filter value and another color to the lowest normalized matched filter value. Computer generated hues are assigned to intermediate values, based upon a linear scale, as above described.
The means 256 projects the generated color map upon the basket surface, based upon location of the nodes in the three dimensional mesh.
FIG. 27 shows a representative display processed according to the above methodology. The CPU 206 generates this display on the display device 246 for viewing by the physician.
The display matches the normalized isoconduction values with the normalized iso-E-Characteristic values, in effect matching electrograms with tissue E-Characteristics. This matching provides more precise differentiation between regions of infarcted tissue and regions of healthy tissue.
This information can be further processed to identify a potential ablation site to maximize the CIR.
(v) Identifying a Potential Ablation Site
FIG. 28 shows a means 258 for identifying a potential ablation site based upon the matched output of the normalized conduction values and the normalized E-Characteristic values, generated by the means 256.
The means 258 selects a threshold value. Tissue regions having matched output values above the threshold constitute potential ablation sites. Locating an optimal threshold value can be done by empirical study or modeling. The threshold value for a given set of data will also depend upon the professional judgment of the physician.
FIG. 29 shows a representative display processed according to the above methodology. In FIG. 29, a threshold of 0.8 has been used for illustration purposes. Values greater than the threshold of 0.8 have been set to 1.0, while values equal to or less than 0.8 have been set to 0.0. The CPU 206 generates this display on the display device 246 for viewing by the physician.
FIG. 29 provides by sharp contrast between black and white (with no intermediate hues) the potential ablation site (Area A).
E. Ablating the Tissue
Regardless of the specific form of the output used, the physician analyses one or more of the outputs derived from the basket electrodes 38 to locate likely efficacious sites for ablation.
The physician can now takes steps to ablate the myocardial tissue areas located by the basket electrodes 38. The physician can accomplish this result by using an electrode to thermally destroy myocardial tissue, either by heating or cooling the tissue. Alternatively, the physician can inject a chemical substance that destroys myocardial tissue. The physician can use other means for destroying myocardial tissue as well.
In the illustrated embodiment (see FIG. 30), an external steerable ablating probe 100 is deployed in association with the basket structure 36.
Various features of the invention are set forth in the following claims.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US4380237 *||Aug 17, 1981||Apr 19, 1983||Massachusetts General Hospital||Apparatus for making cardiac output conductivity measurements|
|US4522212 *||Nov 14, 1983||Jun 11, 1985||Mansfield Scientific, Inc.||Endocardial electrode|
|US4628937 *||Aug 2, 1984||Dec 16, 1986||Cordis Corporation||Mapping electrode assembly|
|US4674518 *||Sep 6, 1985||Jun 23, 1987||Cardiac Pacemakers, Inc.||Method and apparatus for measuring ventricular volume|
|US4682596 *||May 22, 1984||Jul 28, 1987||Cordis Corporation||Electrosurgical catheter and method for vascular applications|
|US4699147 *||Sep 25, 1985||Oct 13, 1987||Cordis Corporation||Intraventricular multielectrode cardial mapping probe and method for using same|
|US4836214 *||Dec 1, 1986||Jun 6, 1989||Bomed Medical Manufacturing, Ltd.||Esophageal electrode array for electrical bioimpedance measurement|
|US4852580 *||Nov 6, 1987||Aug 1, 1989||Axiom Medical, Inc.||Catheter for measuring bioimpedance|
|US4911174 *||Feb 13, 1989||Mar 27, 1990||Cardiac Pacemakers, Inc.||Method for matching the sense length of an impedance measuring catheter to a ventricular chamber|
|US5041973 *||May 1, 1989||Aug 20, 1991||London Health Association||Cardiac mapping system simulator|
|US5058583 *||Jul 13, 1990||Oct 22, 1991||Geddes Leslie A||Multiple monopolar system and method of measuring stroke volume of the heart|
|US5092339 *||Jul 23, 1990||Mar 3, 1992||Geddes Leslie A||Method and apparatus for electrically compensated measurement of cardiac output|
|US5109870 *||Oct 26, 1990||May 5, 1992||Forschungsgesellschaft Fur Biomedizinische Technik E.V.||Apparatus for and method of motility and peristalsis monitoring|
|US5137019 *||Mar 1, 1991||Aug 11, 1992||Cardiac Pacemakers, Inc.||Variation in cardiac chamber volume or pressure as a controlling parameter|
|US5156151 *||Feb 15, 1991||Oct 20, 1992||Cardiac Pathways Corporation||Endocardial mapping and ablation system and catheter probe|
|US5195968 *||Jul 17, 1992||Mar 23, 1993||Ingemar Lundquist||Catheter steering mechanism|
|US5197467 *||Jun 22, 1992||Mar 30, 1993||Telectronics Pacing Systems, Inc.||Multiple parameter rate-responsive cardiac stimulation apparatus|
|US5224475 *||Nov 20, 1991||Jul 6, 1993||Medtronic, Inc.||Method and apparatus for termination of ventricular tachycardia and ventricular fibrillation|
|US5228442 *||Dec 3, 1992||Jul 20, 1993||Cardiac Pathways Corporation||Method for mapping, ablation, and stimulation using an endocardial catheter|
|US5233515 *||Jun 8, 1990||Aug 3, 1993||Cosman Eric R||Real-time graphic display of heat lesioning parameters in a clinical lesion generator system|
|US5239999 *||Jul 24, 1992||Aug 31, 1993||Cardiac Pathways Corporation||Helical endocardial catheter probe|
|US5246008 *||Jan 7, 1992||Sep 21, 1993||Guido Fehling||Method for monitoring a patient for rejection reactions to an implanted heart|
|US5255679 *||Jun 2, 1992||Oct 26, 1993||Cardiac Pathways Corporation||Endocardial catheter for mapping and/or ablation with an expandable basket structure having means for providing selective reinforcement and pressure sensing mechanism for use therewith, and method|
|US5279299 *||Jul 24, 1992||Jan 18, 1994||Cardiac Pathways Corporation||Endocardial mapping and ablation system and catheter probe|
|US5282840 *||Mar 26, 1992||Feb 1, 1994||Medtronic, Inc.||Multiple frequency impedance measurement system|
|US5293869 *||Sep 25, 1992||Mar 15, 1994||Ep Technologies, Inc.||Cardiac probe with dynamic support for maintaining constant surface contact during heart systole and diastole|
|US5297549 *||Sep 23, 1992||Mar 29, 1994||Endocardial Therapeutics, Inc.||Endocardial mapping system|
|US5309910 *||Sep 25, 1992||May 10, 1994||Ep Technologies, Inc.||Cardiac mapping and ablation systems|
|US5313943 *||Sep 25, 1992||May 24, 1994||Ep Technologies, Inc.||Catheters and methods for performing cardiac diagnosis and treatment|
|US5324284 *||Jun 5, 1992||Jun 28, 1994||Cardiac Pathways, Inc.||Endocardial mapping and ablation system utilizing a separately controlled ablation catheter and method|
|US5334193 *||Nov 13, 1992||Aug 2, 1994||American Cardiac Ablation Co., Inc.||Fluid cooled ablation catheter|
|US5341807 *||Jun 30, 1992||Aug 30, 1994||American Cardiac Ablation Co., Inc.||Ablation catheter positioning system|
|US5345936 *||Jun 25, 1993||Sep 13, 1994||Cardiac Pathways Corporation||Apparatus with basket assembly for endocardial mapping|
|US5383917 *||Jul 5, 1991||Jan 24, 1995||Jawahar M. Desai||Device and method for multi-phase radio-frequency ablation|
|US5397339 *||May 7, 1993||Mar 14, 1995||Desai; Jawahar M.||Catheter for mapping and ablation and method therefor|
|US5406946 *||Jan 14, 1994||Apr 18, 1995||Cardiac Pathways Corporation||Endocardial mapping and ablation system and catheter probe and method|
|US5409000 *||Sep 14, 1993||Apr 25, 1995||Cardiac Pathways Corporation||Endocardial mapping and ablation system utilizing separately controlled steerable ablation catheter with ultrasonic imaging capabilities and method|
|US5447529 *||Jan 28, 1994||Sep 5, 1995||Philadelphia Heart Institute||Method of using endocardial impedance for determining electrode-tissue contact, appropriate sites for arrhythmia ablation and tissue heating during ablation|
|1||*||Michael A. Fallert, MD, Myocardial Electrical Impedance Mapping oflschemic Sheep Hearts and Healing Aneurysms, Circulation vol. 87, No. 1 Jan. 1993, 199 207.|
|2||Michael A. Fallert, MD, Myocardial Electrical Impedance Mapping oflschemic Sheep Hearts and Healing Aneurysms, Circulation vol. 87, No. 1 Jan. 1993, 199-207.|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US5954661 *||Mar 31, 1997||Sep 21, 1999||Thomas Jefferson University||Tissue characterization and treatment using pacing|
|US6088614 *||Mar 31, 1997||Jul 11, 2000||Boston Scientific Corporation||Tissue characterization to identify an ablation site|
|US6123702 *||Sep 10, 1998||Sep 26, 2000||Scimed Life Systems, Inc.||Systems and methods for controlling power in an electrosurgical probe|
|US6183468||Sep 10, 1998||Feb 6, 2001||Scimed Life Systems, Inc.||Systems and methods for controlling power in an electrosurgical probe|
|US6245065||Sep 10, 1998||Jun 12, 2001||Scimed Life Systems, Inc.||Systems and methods for controlling power in an electrosurgical probe|
|US6408199||Jul 7, 2000||Jun 18, 2002||Biosense, Inc.||Bipolar mapping of intracardiac potentials with electrode having blood permeable covering|
|US6488679||Jul 26, 2000||Dec 3, 2002||Scimed Life Systems, Inc.||Systems and methods for controlling power in an electrosurgical probe|
|US6494880||Jul 26, 2000||Dec 17, 2002||Scimed Life Systems, Inc.||Systems and methods for controlling power in an electrosurgical probe|
|US6546270||Jul 7, 2000||Apr 8, 2003||Biosense, Inc.||Multi-electrode catheter, system and method|
|US6569160||Jul 7, 2000||May 27, 2003||Biosense, Inc.||System and method for detecting electrode-tissue contact|
|US6629931||Nov 6, 2000||Oct 7, 2003||Medtronic, Inc.||Method and system for measuring a source impedance of at least one cardiac electrical signal in a mammalian heart|
|US6663573||May 31, 2002||Dec 16, 2003||Biosense, Inc.||Bipolar mapping of intracardiac potentials using recessed electrodes|
|US7582084||Nov 22, 2002||Sep 1, 2009||Boston Scientific Scimed, Inc.||Systems and methods for controlling power in an electrosurgical probe|
|US7988639 *||Dec 29, 2006||Aug 2, 2011||St. Jude Medical, Atrial Fibrillation Division, Inc.||System and method for complex geometry modeling of anatomy using multiple surface models|
|US8038625 *||Oct 18, 2011||St. Jude Medical, Atrial Fibrillation Division, Inc.||System and method for three-dimensional mapping of electrophysiology information|
|US8647284||Jul 17, 2012||Feb 11, 2014||St. Jude Medical, Atrial Fibrillation Division, Inc.||System and method for mapping complex fractionated electrogram information|
|US20030199863 *||Nov 22, 2002||Oct 23, 2003||Swanson David K.||Systems and methods for controlling power in an electrosurgical probe|
|US20070073179 *||Sep 15, 2005||Mar 29, 2007||St. Jude Medical, Atrial Fibrillation Division, Inc.||System and Method for Three Dimensional Mapping of Electrophysiology Information|
|US20070270705 *||Dec 29, 2006||Nov 22, 2007||Starks Daniel R||System and method for complex geometry modeling of anatomy using multiple surface models|
|EP1112720A1 *||Dec 29, 1999||Jul 4, 2001||Stockert, Rüdiger||Device for treating biological tissues with high frequency currents|
|International Classification||A61B5/042, A61B5/053, A61B18/14, A61B5/0452|
|Cooperative Classification||A61B2018/126, A61B2562/0209, A61B18/1492, A61B18/14, A61B2018/1253, A61B2562/043, A61B5/0452, A61B5/0422, A61B5/6858, A61B2018/00875, A61B2018/00214, A61B5/6855, A61B2017/003, A61B2018/00761, A61B2018/128, A61B2018/1273, A61B5/0535, A61B2018/00886, A61B2018/124, A61B5/0538, A61B2018/00755|
|European Classification||A61B5/68D1H5, A61B5/68D1H2, A61B5/053N, A61B18/14V, A61B5/0452, A61B5/042D, A61B5/053F|
|Aug 29, 1996||AS||Assignment|
Owner name: EP TECHNOLOGIES, INC., CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:PANESCU, DORIN;SWANSON, DAVID K.;REEL/FRAME:008123/0687
Effective date: 19960722
|May 20, 1997||CC||Certificate of correction|
|Apr 28, 2000||FPAY||Fee payment|
Year of fee payment: 4
|Mar 29, 2004||FPAY||Fee payment|
Year of fee payment: 8
|Apr 17, 2008||FPAY||Fee payment|
Year of fee payment: 12